The present study was undertaken to establish in normal volunteers the alte
rations in beta -cell responsiveness to glucose associated with a constant
infusion of glucagon-like peptide-1 (GLP-1) or a pretreatment infusion for
60 min. A high-dose graded glucose infusion protocol was used to explore th
e dose-response relationship between glucose and insulin secretion. Studies
were performed in 10 normal volunteers, and insulin secretion rates (ISR)
were calculated by deconvolution of peripheral C-peptide levels by use of a
two-compartmental model that utilized mean kinetic parameters. During the
saline study, from 5 to 15 mM glucose, the relationship between glucose and
ISR was linear. Constant GLP-1 infusion (0.4 pmol.kg(-1).min(-1)) shifted
the dose-response curve to the left, with an increase in the slope of this
curve from 5 to 9 mM glucose from 71.0 +/- 12.4 pmol.min(-1).mM(-1) during
the saline study to 241.7 +/- 36.6 pmol.min(-1).mM(-1) during the constant
GLP-1 infusion (P< 0.0001). GLP-1 consistently stimulated a >200% increase
in ISR at each 1 mM glucose interval, maintaining plasma glucose at,10 mM (
P< 0.0007). Pretreatment with GLP-1 for 60 min resulted in no significant p
riming of the <beta>-cell response to glucose (P = 0.2). Insulin clearance
rates were similar in all three studies at corresponding insulin levels. Th
ese studies demonstrate that physiological levels of GLP-1 stimulate glucos
e-induced insulin secretion in a linear manner, with a consistent increase
in ISR at each 1 mM glucose interval, and that they have no independent eff
ect on insulin clearance and no priming effect on subsequent insulin secret
ory response to glucose.